CAS Number86-74-8
Synonymsdiphenylenimine; DIPHENYLIMIDE; Carbazole; polycarbazole; 2-(2-Bromoanilino)pyridine; Diphenylimid; 9H-CARBAZOLE; Dibenzopyrrol; EINECS 201-696-0; 'LGC' (2409); usafek-600; dibenzopyrrole; 9-AZAFLUORENE; MFCD00004960
Molecular FormulaC12H9N
Molecular Weight167.21
Purity≥95 (GC)%
Density1.1
Boiling Point355 °C (lit.)
Melting Point243-246 °C (lit.)
Appearancepowder
EINECS201-696-0
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 86-74-8 |
| Catalog No. | 2A-9013998 |
| Chinese Name | 咔唑 |
| Synonyms | diphenylenimine; DIPHENYLIMIDE; Carbazole; polycarbazole; 2-(2-Bromoanilino)pyridine; Diphenylimid; 9H-CARBAZOLE; Dibenzopyrrol; EINECS 201-696-0; 'LGC' (2409); usafek-600; dibenzopyrrole; 9-AZAFLUORENE; MFCD00004960 |
| Molecular Formula | C12H9N |
| Molecular Weight | 167.21 |
| Purity | ≥95 (GC) |
| Density | 1.1 |
| Boiling Point | 355 °C (lit.) |
| Melting Point | 243-246 °C (lit.) |
| Appearance | powder |
| Water Solubility | <0.1 g/100 mL at 19 ºC |
| Storage Condition | This product should be sealed and stored in a cool |
| Packaging | III |
| Application | Carbazole is a tricyclic aromatic heterocyclic compound. Carbazole can form a new type of DNA microgroove complex and inhibit the synthesis of new DNA or RNA [1]. |
| EINECS | 201-696-0 |
| HTC | 2933990090 |
| PubChem ID | 24892756 |
| MDL Number | MFCD00004960 |
| SMILES | c1ccc2c(c1)[nH]c3ccccc23 |
| InChI | 1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H |
| InChI Key | UJOBWOGCFQCDNV-UHFFFAOYSA-N |
| Beilstein/REAXYS | 3956 |
| NACRES Code | NA.47 |
| UNSPSC | 12171500 |
| Hazard Symbols | 9 |
| MSDS | msds/13998_1_86_74_8.pdf |
| Bioactivity | Carbazole is a tricyclic aromatic heterocyclic. Carbazole can form a new type of DNA minor groove complex to suppress the synthesis of new DNA or RNA[1]. Related Catalog Signaling Pathways >> Cell Cycle/DNA Damage >> DNA/RNA Synthesis Research Areas >> Others References [1]. F A Tanious, et al. A new type of DNA minor-groove complex: carbazole dication-DNA interactions. Biochemistry. 1997 Dec 9;36(49):15315-25. [2]. carbazole and its derivatives as antitumor agents. Anticancer Agents Med Chem. 2015;15(8):1049-65. [3]. Kai Lin Woon, et al. Effect of conjugation and aromaticity of 3,6 di-substituted carbazoles on triplet energy and the implication of triplet energy in multiple-cyclic aromatic compounds. RSC Adv., 2018, 8, 9850-9857. Chemical & Physical Properties Density 1.1 Boiling Point 355.0±11.0 °C at 760 mmHg Melting Point 243-246 °C(lit.) Molecular Formula C12H9N Molecular Weight 167.207 Flash Point 220 ºC Exact Mass 167.073502 PSA 15.79000 LogP 3.72 Vapour Pressure 0.0±0.8 mmHg at 25°C Index of Refraction 1.768 InChIKey UJOBWOGCFQCDNV-UHFFFAOYSA-N SMILES c1ccc2c(c1)[nH]c1ccccc12 Stability Stable. Combustible. Incompatible with strong oxidizing agents, nitrogen oxides, potassium hydroxide. Water Solubility <0.1 g/100 mL at 19 ºC |
| Use of | Carbazole is a tricyclic aromatic heterocyclic. Carbazole can form a new type of DNA minor groove complex to suppress the synthesis of new DNA or RNA[1]. Properties Articles53 Name 9H-carbazole Synonym More Synonyms Carbazole Biological Activity Description Carbazole is a tricyclic aromatic heterocyclic. Carbazole can form a new type of DNA minor groove complex to suppress the synthesis of new DNA or RNA[1]. Related Catalog Signaling Pathways >> Cell Cycle/DNA Damage >> DNA/RNA Synthesis Research Areas >> Others References [1]. F A Tanious, et al. A new type of DNA minor-groove complex: carbazole dication-DNA interactions. Biochemistry. 1997 Dec 9;36(49):15315-25. [2]. carbazole and its derivatives as antitumor agents. Anticancer Agents Med Chem. 2015;15(8):1049-65. [3]. Kai Lin Woon, et al. Effect of conjugation and aromaticity of 3,6 di-substituted carbazoles on triplet energy and the implication of triplet energy in multiple-cyclic aromatic compounds. RSC Adv., 2018, 8, 9850-9857. Chemical & Physical Properties Molecular Formula C12H9N Exact Mass 167.073502 PSA 15.79000 Index of Refraction 1.768 InChIKey UJOBWOGCFQCDNV-UHFFFAOYSA-N Stability Stable. Combustible. Incompatible with strong oxidizing agents, nitrogen oxides, potassium hydroxide. |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 20.0% |
| Transport Info | Product name: Chemical name |
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